Ramachandran Ramya Devi

Crystallin gene mutations in Indian families with inherited pediatric cataract.

Ramachandran Ramya Devi, Wenliang Yao, P Vijayalakshmi et al. · PubMed · 2008 · 158 citations

Novel mutations in GJA8 associated with autosomal dominant congenital cataract and microcornea.

Ramachandran Ramya Devi, P Vijayalakshmi · PubMed · 2006 · 84 citations

Novel mutations in GJA3 associated with autosomal dominant congenital cataract in the Indian population.

Ramachandran Ramya Devi, Reena Chandrashekar, P Vijayalakshmi · PubMed · 2005 · 48 citations